Impact of genetic similarity on imputation accuracy Nab Raj Roshyara1,2 * and Markus Scholz1,2 Background: Genotype imputation is a common technique in genetic research. Genetic similarity between target population and reference dataset is crucial for high-quality results. Although several reference panels are available, it is often not clear which is the most optimal for a particular target dataset to be imputed. Maximizing genetic similarity between study sample and intended reference panels may be the straight forward method for selecting the genetically best-matched reference. However, the impact of genetic similarity on imputation accuracy has not yet been studied in detail. Results: We performed a simulation study in 20 ethnic groups ...
A current approach to mapping complex-disease-susceptibility loci in genome-wide association (GWA) s...
<div><p>Genotype imputation, used in genome-wide association studies to expand coverage of single nu...
Genotype imputation, used in genome-wide association studies to expand coverage of single nucleotide...
Imputation, the process of inferring genotypes for untyped variants, is used to identify and refine ...
Genome-wide association studies have successfully identified common variants that are associated wit...
Samoa is a population isolate that has generated a unique genetic profile by means of the founder ef...
Imputation using the 1000 Genomes haplotype reference panel has been widely adapted to estimate geno...
Genotype imputation is an important tool in human genetics studies, which uses reference sets with k...
Genotype imputation is widely used to enrich genetic datasets. The operation relies on panels of kno...
<div><p>Genotype imputation is an important tool in human genetics studies, which uses reference set...
Genetic imputation is a cost-efficient way to improve the power and resolution of genome-wide associ...
BACKGROUND: Imputation of missing genotypes is becoming a very popular solution for synchronizing ge...
Imputation is a method of predicting unknown genotypes in a dataset by comparing measured genotypes ...
A variety of modern software packages are available for genotype imputation relying on advanced conc...
Imputation using the 1000 Genomes haplotype reference panel has been widely adapted to estimate geno...
A current approach to mapping complex-disease-susceptibility loci in genome-wide association (GWA) s...
<div><p>Genotype imputation, used in genome-wide association studies to expand coverage of single nu...
Genotype imputation, used in genome-wide association studies to expand coverage of single nucleotide...
Imputation, the process of inferring genotypes for untyped variants, is used to identify and refine ...
Genome-wide association studies have successfully identified common variants that are associated wit...
Samoa is a population isolate that has generated a unique genetic profile by means of the founder ef...
Imputation using the 1000 Genomes haplotype reference panel has been widely adapted to estimate geno...
Genotype imputation is an important tool in human genetics studies, which uses reference sets with k...
Genotype imputation is widely used to enrich genetic datasets. The operation relies on panels of kno...
<div><p>Genotype imputation is an important tool in human genetics studies, which uses reference set...
Genetic imputation is a cost-efficient way to improve the power and resolution of genome-wide associ...
BACKGROUND: Imputation of missing genotypes is becoming a very popular solution for synchronizing ge...
Imputation is a method of predicting unknown genotypes in a dataset by comparing measured genotypes ...
A variety of modern software packages are available for genotype imputation relying on advanced conc...
Imputation using the 1000 Genomes haplotype reference panel has been widely adapted to estimate geno...
A current approach to mapping complex-disease-susceptibility loci in genome-wide association (GWA) s...
<div><p>Genotype imputation, used in genome-wide association studies to expand coverage of single nu...
Genotype imputation, used in genome-wide association studies to expand coverage of single nucleotide...